Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency.
We investigated the peroxisomal beta-oxidation system in liver from a patient with clinical features similar to those in the cerebrohepatorenal (Zellweger) syndrome and with elevated levels in body fluids of very-long-chain fatty acids and intermediates in the biosynthesis of bile acids. The peroxis...
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| Pubblicato in: | Proc Natl Acad Sci U S A |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
National Academy of Sciences
1987
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC304678/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2882519/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.84.8.2494 |
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